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Effects of Ciprofol versus Etomidate on Hemodynamics During Double-Lumen Endobronchial Intubation in Elderly Patients Undergoing Thoracoscopic Surgery: A Randomized, Controlled, Double-Blind Trial

Effects of Ciprofol versus Etomidate on Hemodynamics During Double-Lumen Endobronchial Intubation in Elderly Patients Undergoing Thoracoscopic Surgery: A Randomized, Controlled, Double-Blind Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116554
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-12
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thoracoscopic surgery

Interventions

Etomidate Group (Group E):Anesthesia induction with etomidate
Ciprofol Group (Group C) :Anesthesia induction with ciprofol

Sponsors

Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients aged 65 or above. 2. ASA classification is grade I to III. 3. Those who are scheduled to undergo thoracoscopic surgery under general anesthesia (such as lobectomy/segmentectomy, bullae resection, pleural biopsy, etc.) and plan for single-lung ventilation with double-lumen bronchial intubation. 4. The patient or his/her legal representative gives informed consent and signs a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with expected difficult airways (Modified Markov Scale score >= grade III, or with other clear indications of difficult airways). 2. Severe cardiovascular and cerebrovascular diseases: There has been a history of unstable angina pectoris or myocardial infarction within the past six months. NYHA cardiac function classification > or = Grade III, or left ventricular ejection fraction 30 kg/m ² or < 18 kg/m ². 7. The researcher determines that there are other circumstances that make participation in this study unsuitable (such as mental illness, communication disorders, etc.).

Design outcomes

Primary

MeasureTime frame
MAP change value during induction of general anesthesia;HR change value during induction of general anesthesia;

Secondary

MeasureTime frame
Use of vasoactive drugs;Incidence of cardiovascular adverse events;Glucose;Lactic acid;

Countries

China

Contacts

Public ContactJinli Wu

Affiliated Hospital of Guizhou Medical University

534160489@qq.com+86 189 8510 0136

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026